A CRYSTALLOGRAPHIC MAP OF CHIRAL RECOGNITION IN PI-COMPLEXES OF AROMATIC-ALDEHYDES AND A CHIRAL TRANSITION-METAL LEWIS-ACID - ENANTIOFACE BINDING SELECTIVITIES IN SOLUTION CORRELATE TO DISTANCES BETWEEN METAL AND CARBON STEREOCENTERS IN THE SOLID-STATE
被引:7
作者:
BOONE, BJ
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UNIV UTAH,DEPT CHEM,SALT LAKE CITY,UT 84112UNIV UTAH,DEPT CHEM,SALT LAKE CITY,UT 84112
BOONE, BJ
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KLEIN, DP
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UNIV UTAH,DEPT CHEM,SALT LAKE CITY,UT 84112UNIV UTAH,DEPT CHEM,SALT LAKE CITY,UT 84112
KLEIN, DP
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MENDEZ, NQ
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UNIV UTAH,DEPT CHEM,SALT LAKE CITY,UT 84112UNIV UTAH,DEPT CHEM,SALT LAKE CITY,UT 84112
MENDEZ, NQ
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SEYLER, JW
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UNIV UTAH,DEPT CHEM,SALT LAKE CITY,UT 84112UNIV UTAH,DEPT CHEM,SALT LAKE CITY,UT 84112
SEYLER, JW
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ARIF, AM
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UNIV UTAH,DEPT CHEM,SALT LAKE CITY,UT 84112UNIV UTAH,DEPT CHEM,SALT LAKE CITY,UT 84112
ARIF, AM
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GLADYSZ, JA
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UNIV UTAH,DEPT CHEM,SALT LAKE CITY,UT 84112UNIV UTAH,DEPT CHEM,SALT LAKE CITY,UT 84112
The title claim is established with five pi-aromatic aldehyde complexes [(eta(5)-C5H5)Re(NO)(PPh(3))(eta(2)-O=CHAr)](+) X(-); electronegative aryl substituents give shorter rhenium-carbon bond lengths and higher binding selectivities, providing the first easily conceptualized mechanism for an electronic effect upon chiral recognition.